Molecular testing in congenital adrenal hyperplasia due to 21α-hydroxylase deficiency in the era of newborn screening
Sarafoglou, K, Lorentz, C P, Otten, N, Oetting, W S, Grebe, S K G
Published in Clinical genetics (01.07.2012)
Published in Clinical genetics (01.07.2012)
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Journal Article
Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3Mb
Adeyinka, Adewale, Stockero, Kimberly J., Flynn, Heather C., Lorentz, Cindy P., Ketterling, Rhett P., Jalal, Syed M.
Published in Genetics in medicine (01.11.2004)
Published in Genetics in medicine (01.11.2004)
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Journal Article
Microduplication 22q11.2, an Emerging Syndrome: Clinical, Cytogenetic, and Molecular Analysis of Thirteen Patients
Ensenauer, Regina E., Adeyinka, Adewale, Flynn, Heather C., Michels, Virginia V., Lindor, Noralane M., Dawson, D. Brian, Thorland, Erik C., Lorentz, Cindy Pham, Goldstein, Jennifer L., McDonald, Marie T., Smith, Wendy E., Simon-Fayard, Elba, Alexander, Alan A., Kulharya, Anita S., Ketterling, Rhett P., Clark, Robin D., Jalal, Syed M.
Published in American journal of human genetics (01.11.2003)
Published in American journal of human genetics (01.11.2003)
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Journal Article
Subtelomere deletions and translocations are frequently familial
Adeyinka, Adewale, Adams, S. Annie, Lorentz, Cindy P., Van Dyke, Daniel L., Jalal, Syed M.
Published in American journal of medical genetics. Part A (15.05.2005)
Published in American journal of medical genetics. Part A (15.05.2005)
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Journal Article
Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients
Jalal, Syed M., Harwood, Aaron R., Sekhon, Gurbax S., Lorentz, Cindy Pham, Ketterling, Rhett P., Babovic-Vuksanovic, Dusica, Meyer, Reid G., Ensenauer, Regina, Anderson, Marvin H., Michels, Virginia V.
Published in Genetics in medicine (01.01.2003)
Published in Genetics in medicine (01.01.2003)
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